Hutchinson-Gilford progeria syndrome (HGPS), an extremely rare genetic disorder, arises when a silent point mutation in the gene encoding the nuclear envelope protein lamin A, LMNA, leads to abnormal ...
Children who develop deep wrinkles, stunted growth, and rapidly aging bones and blood vessels as early as 1 to 2 years of age may be suffering from Hutchinson-Gilford Progeria Syndrome (HGPS), a rare ...
Sentynl, a Zydus Group company, receives worldwide proprietary rights to Zokinvy, adding to portfolio of biopharmaceuticals for rare and ultra-rare diseases Zokinvy is approved in the U.S. (2020), ...
“The findings highlight miRNA-145-5p and miRNA-27b-3p as potential therapeutic targets to address adipose tissue defects and premature aging in HGPS” “The findings highlight miRNA-145-5p and miRNA-27b ...
Researchers discovered that a longevity gene from centenarians can reverse heart damage linked to progeria, suggesting a new approach to treating rapid and age-related heart aging. A major advancement ...
Learn about Progeria, a rare genetic disorder causing premature ageing in children—explore symptoms, diagnosis, treatment ...
The Nature Index 2025 Research Leaders — previously known as Annual Tables — reveal the leading institutions and countries/territories in the natural and health sciences, according to their output in ...
Researchers from the University of Bristol and IRCCS MultiMedica showed that a gene linked to supercentenarians’ longevity can counter heart damage in Hutchinson-Gilford Progeria Syndrome.
A woman suffering from a rare 'Benjamin Button' condition has defied doctors' predictions of an early grave. Tiffany Wedekind from Columbus, Ohio, suffers from Hutchinson-Gilford progeria syndrome, ...
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